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uMR 780 Magnetic Resonance Imaging System - Indonesia BPOM Medical Device Registration

uMR 780 Magnetic Resonance Imaging System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501819092. The device is manufactured by SHANGHAI UNITED IMAGING HEALTHCARE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is D&V INTERNATIONAL PROSPERS SCINTILLATING.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
uMR 780 Magnetic Resonance Imaging System
Analysis ID: AKL 21501819092

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

AR Address

Foresta Business Loft 3 No. 1 Jln. BSD Boulevard Utara, BSD City Desa Lengkong Kulon, Kec. Pagedangan, Kab. Tangerang - Banten, 15331

Registration Date

Sep 05, 2023

Expiry Date

Jul 27, 2028

Product Type

Diagnostic Radiology Equipment

Magnetic resonance diagnostic device.

Non Radiation Electromedics

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